[具有 SWI/SNF 复合物缺失的胃甲胎蛋白腺癌的临床病理特征]。

J Z Yang, X X Guo, C Xu, Y Y Hou, W Yuan
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引用次数: 0

摘要

目的研究SWI/SNF复合体缺失的胃甲胎蛋白(AFP)腺癌的临床病理特征和治疗方法。方法收集2021年1月至2022年12月在复旦大学附属中山医院确诊的4例伴SWI/SNF复合体缺失的胃甲胎蛋白(AFP)腺癌病例,总结其组织形态学特征、免疫组化(IHC)、Epstein-Barr病毒编码RNA(EBER)原位杂交、新一代测序结果、临床病理特征及治疗方法,并进行文献回顾。结果4 名患者中,3 男 1 女。他们表现为腹痛、嗳气和腹泻。三名患者的血清甲胎蛋白明显升高,内镜检查显示有溃疡性病变。显微镜下,肿瘤细胞主要呈弥漫性片状或巢状生长,具有典型的肝样腺癌特征。有两个病例出现腺样增生,这些区域的肿瘤细胞具有清晰的细胞质,提示为肠母细胞分化。肿瘤细胞核呈多形性,核仁大,有快速有丝分裂。IHC 结果显示,肿瘤细胞表达 AFP、GPC3 和 SALL4,广谱角蛋白(CKpan)和 E-cadherin也有保留表达。对 SWI/SNF 复合物亚基,即 INI1(SMARCB1)、BRG1(SMARCA4)、BRM(SMARCA2)和 ARID1A 蛋白进行了 IHC 检测。在所有四个病例中,肝样腺癌区域和肠细胞分化区域均出现了SMARCA2缺失,其中一个肠细胞分化病例还出现了ARID1A缺失。未见SMARCB1和SMARCA4缺失。四例病例的p53蛋白均呈弥漫阳性,Ki-67增殖指数为80%-90%。未检测到错配修复缺失;其中一个病例显示HER2强阳性(3+),EBER阴性。通过新一代测序,四例患者均未检测到 SWI/SNF 复合物相关亚基的突变。四名患者中,两人在手术时因远处转移而接受了姑息手术,两人接受了根治性切除术。三名患者接受了术后辅助化疗。结论AFP生成腺癌是胃癌的一种罕见亚型,可合并SWI/SNF复合体缺失,其病理形态学表现不同于经典的SWI/SNF复合体缺失的未分化癌,具有横纹肌样表型。
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[Clinicopathological features of gastric alpha-fetoprotein-producing adenocarcinoma with SWI/SNF complex deletion].

Objective: To investigate the clinicopathological features and treatment of gastric alpha-fetoprotein (AFP)-producing adenocarcinoma with SWI/SNF complex deletion. Methods: Four cases of gastric AFP-producing adenocarcinoma with SWI/SNF complex deletion diagnosed in Zhongshan Hospital of Fudan University from January 2021 to December 2022 were collected, and their histomorphological characteristics, immunohistochemical (IHC), in situ hybridization of Epstein-Barr virus-encoded RNA (EBER), next-generation sequencing results, clinicopathological features and treatment were summarized, and literature review was conducted. Results: Among the 4 patients, there were three males and one female. They presented with abdominal pain, belching and melena. Serum AFP was significantly elevated in three patients, and endoscopy showed ulcerative lesions. Microscopically, the tumor cells showed mainly diffuse flaky or nest-like growth and typical characteristics of hepatoid adenocarcinoma. In two cases there were adenoid growth, and the tumor cells in these areas possessed clear cytoplasm, suggesting enteroblastic differentiation. The tumor cell nuclei were pleomorphic with large nucleoli and brisk mitoses. The IHC results showed that the tumor cells expressed AFP, GPC3 and SALL4, and there was retained expression of broad-spectrum keratin (CKpan) and E-cadherin. IHC detection of SWI/SNF complex subunits, namely INI1 (SMARCB1), BRG1 (SMARCA4), BRM (SMARCA2), ARID1A protein was performed. In all four cases the hepatoid adenocarcinoma region and enteroblastic differentiation region showed SMARCA2 deletion, and one case with enteroblastic differentiation also showed ARID1A deletion. SMARCB1 and SMARCA4 deletions were not seen. All the four cases were diffusely positive for p53 protein, and the Ki-67 proliferation index was 80%-90%. There were no mismatch repair deletion detected; one cases showed HER2 was strongly positive (3+), and EBER was negative. None of the four cases had mutations in the SWI/SNF complex-related subunits detected by next-generation sequencing. Among the four patients, two underwent palliative surgery due to distant metastasis at the time of surgery, two underwent radical resection. Postoperative adjuvant chemotherapy was given to three patients. Conclusions: AFP-producing adenocarcinoma is a rare subtype of gastric cancer, which can be combined with SWI/SNF complex deletion, and the pathomorphological manifestations are different from the classical SWI/SNF complex deletion of undifferentiated carcinoma with rhabdoid phenotype.

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中华病理学杂志
中华病理学杂志 Medicine-Medicine (all)
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